Escherichia coli Group 2 capsules and their interplay with bacteriophages.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-09-18 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1588121
Naoise McGarry, Catherine Toner-Bartelds, Stephen G J Smith
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Abstract

Introduction: Extracellular polysaccharide capsules of Gram-negative bacteria, such as Escherichia coli (E. coli), mediate interactions with host defences and bacteriophages (phages). Capsules may act as barriers to infection or serve as essential receptors when phages rely on capsule recognition and degradation by depolymerases.

Methods: In this study, we examined the Group 2 K2 capsule of the extra-intestinal pathogenic E. coli (ExPEC) prototype CFT073 to determine its role in phage infection. We assessed whether the capsule acts as a barrier or receptor and explored the effect of temperature on such interactions. Additionally, we analysed E. coli genomes to identify whether capsule biosynthesis genes were co-located with other loci associated with phage defence. The evolutionary context of these associations was alsoc explored.

Results: The K2 capsule of CFT073 exhibited dual functionality, acting both as a barrier to phage infection and as a receptor facilitating infection. A previously unrecognized synergy was observed between capsule expression and a type IV toxin-antitoxin (TA) system in CFT073. It was also shown that co-localisation of capsule and TA loci was present in more than 500 E. coli genomes, indicating a conserved association. Further, these systems were shown to be horizontally co-acquired on a common pathogenicity island.

Discussion: These findings highlight the complex role of capsules in phage interactions and suggest that their functional linkage with TA systems may enhance bacterial persistence. The conserved co-acquisition of these loci on pathogenicity islands underscores their potential importance in the evolution and success of ExPEC pathogens.

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大肠杆菌2组胶囊及其与噬菌体的相互作用。
革兰氏阴性菌(如大肠杆菌)的胞外多糖胶囊介导与宿主防御和噬菌体(噬菌体)的相互作用。当噬菌体依赖于胶囊的识别和解聚合酶的降解时,胶囊可以作为感染的屏障或必不可少的受体。方法:本研究对肠外致病性大肠杆菌(exic)原型CFT073的2组K2胶囊进行检测,以确定其在噬菌体感染中的作用。我们评估了胶囊是作为屏障还是受体,并探讨了温度对这种相互作用的影响。此外,我们分析了大肠杆菌基因组,以确定胶囊生物合成基因是否与其他与噬菌体防御相关的基因座共定位。还探讨了这些关联的进化背景。结果:CFT073的K2胶囊具有双重功能,既可作为噬菌体感染的屏障,又可作为促进感染的受体。在CFT073中,在胶囊表达和IV型毒素-抗毒素(TA)系统之间观察到一种以前未被认识到的协同作用。研究还表明,胶囊位点和TA位点共定位存在于500多个大肠杆菌基因组中,表明它们之间存在保守关联。此外,这些系统被证明是在一个共同的致病性岛上水平共同获得的。讨论:这些发现强调了胶囊在噬菌体相互作用中的复杂作用,并表明它们与TA系统的功能联系可能增强细菌的持久性。这些基因座在致病性岛屿上的保守共同获得强调了它们在exp病原体进化和成功中的潜在重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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